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Travoprost

TRAVATAN Z

Pronunciation: TRA-voe-prost

Travoprost ballicule: receptor binding, kinetics and half-life diagram
Mechanism of action: Travoprost ballicule

What it isProstaglandin FP-receptor agonist increasing uveoscleral outflow; open-angle glaucoma and ocular hypertension.

Why this oneThe branded formulation avoids benzalkonium chloride, which can help when ocular-surface irritation limits other drops.

What limits itIris darkening may be permanent; eyelash growth, periocular change, and conjunctival hyperemia are common local effects.

Travoprost molecular structure (skeletal formula)
Molecular structure: Travoprost

FDA-approved for

FDA label

FDA dosingPopulationStartTargetMax
Elevated IOP in open-angle glaucoma or ocular hypertensionAdults1 drop in affected eye(s) QHS (evening)1 drop QD (evening)1 drop QD

Renal Studied in renal impairment; no clinically relevant changes observed

Hepatic Studied in hepatic impairment; no clinically relevant changes observed

More frequent than once-daily administration may decrease the IOP-lowering effect

Instructions

Available strengths

Cautions

Adverse reactions

Pregnancy No adequate human studies; animal embryo-fetal lethality, abortion, and premature delivery at clinically relevant doses; use only if benefit justifies risk

Lactation Unknown if present in human milk; excreted in rat milk

Cost

Travoprost (TRAVATAN Z)
Strength#/mogeneric $/unitCostPlus
0.004 %dropsper unitnot offered
NADAC is a voluntary CMS survey of what retail community pharmacies pay for the drugs they stock. Travoprost is dispensed outside retail pharmacies, so it rarely appears on surveyed invoices.

Generic entry2013

NO BOXED WARNINGS

Principal riskPermanent iris darkening

Classes and tags

Clinical profile

Therapeutic safety burden0 / 4
Overdose danger0 / 4
Weight-gain liability0 / 4
Sedation liability0 / 4
QT / Torsades0 / 4
Direct muscarinic antagonism0 / 4
Embryofetal risk0 / 4

Legacy pregnancy categoryUnknown / historical label unavailable

Defining liabilityLocal irritation, sensitization or administration-site injury; negligible systemic toxicity at usual use.

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